US4698369A - Flexible, flame-retardant polyurethane foams - Google Patents

Flexible, flame-retardant polyurethane foams Download PDF

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US4698369A
US4698369A US06/875,705 US87570586A US4698369A US 4698369 A US4698369 A US 4698369A US 87570586 A US87570586 A US 87570586A US 4698369 A US4698369 A US 4698369A
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foam
expandable graphite
graphite
reaction mixture
forming reaction
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Raymond W. H. Bell
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DUNLOPILLO Ltd
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Dunlop Ltd
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/02—Elements
    • C08K3/04—Carbon
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S521/00—Synthetic resins or natural rubbers -- part of the class 520 series
    • Y10S521/906—Polyurethane cellular product containing unreacted flame-retardant material

Definitions

  • This invention relates to a method for the production of flexible, flame-retardant polyurethane foams and to novel foams obtained thereby.
  • flexible as used herein includes, but is not restricted to, the categories of foams known to those skilled in the art as “low-resilience”, “conventional” and “high-resilience” foams.
  • Flexible cellular materials have been interpreted by the International Standards Organisation (I,S.O.) TC.45 (Cellular Plastics Committee) as "Cellular polymeric materials capable of significant deflection and recovery or used in applications requiring significant deflection and recovery.”
  • polyurethane foams make them useful for a wide variety of applications, including upholstery and bedding.
  • polyurethane foams are inherently flammable and this leads to melting and spread of burning debris and (in the case of "conventional” foams) may also lead to the sustaining of combustion by progressive smouldering even after the actual flames have extinguished.
  • the object of this invention is to make flexible polyurethane foams behave more like rigid foams and thus produce a protective char with little or no burning melt or drips. This is achieved by including a particular type of graphite in the foam-forming reaction mixture.
  • a flexible flame-retardant polyurethane foam comprises the reaction product of a polymeric polyol and an organic polyisocyanate characterised in that the foam contains expandable graphite as hereinafter defined.
  • the conditions needed to produce a flexible foam will vary according to the reactants selected. A person of ordinary skill in the art will know whether to include additives eg a catalyst or a blowing agent and what reaction conditions are required.
  • the molecular weights of the polymeric polyols used in flexible foam manufacture are usually from 1000 to 10,000, preferably from 3000 to 7000, with a functionality of up to 4, preferably 2 to 3.
  • the functionality of the polyisocyanate is usually at least 2.
  • expandable graphite graphite containing one or more exfoliating agents such that considerable expansion will occur at high temperatures.
  • the foam-forming reaction mixture usually contains graphite in an amount such that there will be at least 10% by weight, preferably at least 15% by weight and advantageously at least 25% by weight of graphite in the final foam.
  • the amount of graphite required will depend upon the degree of flame retardance required of the foam but usually the amount of graphite will not exceed 30% by weight in the final foam.
  • the graphite may comprise the sole flame-retardant additive in the foam-forming reaction mixture.
  • flame-retardant ingredients known per se, may be used in addition to the graphite.
  • examples of such ingredients include the hydrated aluminas (eg BACO* FRF 40) and halogen and/or phosphorus-containing compounds, or antimony oxides, or boron-containing compounds.
  • intumescent-generating ingredients eg ammonium polyphosphates
  • intumescent-generating ingredients eg ammonium polyphosphates
  • the foams produced according to the present invention will pass the burning test described in the British Standard specification No. 4735 September 1974.
  • the foams of the present invention are sufficiently flame-retardant that if used with selected textile cover materials the resulting combinations would pass the No. 4 crib test of the British Standard specification BS 5852: Part 2: 1982, preferably the No. 5 crib test, more preferably the No. 6 crib test and advantageously the No. 7 crib test.
  • the No. 7 crib test In view of the varying degree of flammability of different textile materials it is impossible to give absolute directions as to which textile materials are to be selected.
  • a person of ordinary skill in the art would know which materials are likely to be suitable and simple trial and error would then establish whether they were indeed suitable.
  • In order to prepare a foam capable of passing the No. 7 crib test it would generally be necessary for the amount of expendable graphite in the foam to be at least 25% by weight.
  • Free-rise, low-resilience polyurethane foams were made from the formulations shown in TABLE A (overleaf). (Quantities are parts by weight).
  • CONTROL X Average burn length 125 mm in 121 seconds, i.e. the whole sample was burnt.
  • CONTROL Y The addition of alumina hydrate gave only a slight improvement, the average burn length of this sample being 125 mm in 159 seconds.
  • EXAMPLE 1 Average burn length using 40 php fine-grade graphite was 38 mm in 113 seconds. The foam charred (as opposed to the foam of the two CONTROL examples which melted and dripped).
  • EXAMPLE 2 Reduction of the polybutene level and of the graphite level to 8.5 php and 20 php respectively led to an average burn length of 40 mm in 133 seconds.
  • EXAMPLE 3 Substitution of coarse-grade graphite (20 php) in the formulation of EXAMPLE 2 produced an average burn length of 42 mm in 120 seconds, i.e. not significantly different from that of EXAMPLE 2.
  • EXAMPLE 4 A No. 4 crib was placed directly on the top surface of the moulding and ignited.
  • EXAMPLE 5 As EXAMPLE 4, but with No. 5 crib.
  • EXAMPLE 6 As EXAMPLE 4, but with No. 6 crib.
  • High-resilience foams were made by moulding the formulations shown in TABLES C and D (below) in a mould at 50° C., followed by curing for 10 minutes at room temperature. (Quantities are parts by weight).
  • High-resilience foams were made by including formulations as shown in Table E in a mould at 45° C. followed by curing for 10 minutes at room temperature. (Quantities are parts by weight).
  • foam was tested in combination with a woollen fabric of weight approximately 400 g/m 2 using a No. 6 wooden crib (weight 60 g) according to BS 5852 Part 2, 1982. Flaming of the foam/fabric combination ceased 11.5 minutes from the ignition of the wooden crib and there was no progressive smouldering revealed by examination one hour after ignition. The weight loss shown by the foam component was about 3%.
  • Example 10 foam was tested in combination with a wool moquette fabric of weight approximately 800 g/m 2 using a No. 7 wooden crib (weight 120 g) according to BS 5852 Part 2 1982. Flaming of the foam/fabric combination ceased 15 minutes from ignition of the crib. There was no progressive smouldering.
  • a conventional polyether polyurethane foam similar to those described in EXAMPLES 4 to 6 but containing 30% by weight of graphite and having a foam density of 36 Kg/m 3 , was tested in the F.A.A. Kerosene Burner Test* in combination with a 100% wool face fabric and a partially-carbonised viscose interliner. It was found that this combination self-extinguished 3.5 minutes after the commencement of the test and that the overall weight loss was 6.8%.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

Flexible polyurethane foams are used for a wide variety of applications including upholstery and bedding. Unfortunately polyurethane foams are inherently flammable. The invention overcomes this problem by using expandable graphite in the polyurethane foam-forming reaction mixture to improve the burning characteristics of the final foam. Expandable graphite is graphite containing one or more exfoliating agents so that considerable expansion will occur at high temperatures.

Description

This invention relates to a method for the production of flexible, flame-retardant polyurethane foams and to novel foams obtained thereby.
The term "flexible" as used herein includes, but is not restricted to, the categories of foams known to those skilled in the art as "low-resilience", "conventional" and "high-resilience" foams. Flexible cellular materials have been interpreted by the International Standards Organisation (I,S.O.) TC.45 (Cellular Plastics Committee) as "Cellular polymeric materials capable of significant deflection and recovery or used in applications requiring significant deflection and recovery."
The physical and mechanical properties of polyurethane foams make them useful for a wide variety of applications, including upholstery and bedding. However, polyurethane foams are inherently flammable and this leads to melting and spread of burning debris and (in the case of "conventional" foams) may also lead to the sustaining of combustion by progressive smouldering even after the actual flames have extinguished.
It is considered that cellular materials manufactured from flammable polymers are more flammable than the solid materials because the insulating effect of their cellular nature allows a rapid build-up of heat at the heating surface with a consequence high rate of pyrolysis. In solid materials this heat build-up is at a lower rate because of the higher conductivity of the solid material. Although rigid foams have similar thermal conductivity behaviour to flexible foams, the high cross-linked nature of their chemical structure makes them less flammable as polymers and also inherently more inclined to form a protective char rather than to form the flaming molten polymer droplets which occur with flexible foams. Thus both solid and rigid cellular materials burn less easily than flexible foams and are easier to extinguish.
The object of this invention is to make flexible polyurethane foams behave more like rigid foams and thus produce a protective char with little or no burning melt or drips. This is achieved by including a particular type of graphite in the foam-forming reaction mixture.
According to one aspect of the present invention there is provided a method for the production of a flexible flame-retardant polyurethane foam from a foam-forming reaction mixture including a polymeric polyol and an organic polyisocyanate characterised in that the foam-forming reaction mixture also contains expandable graphite as hereinafter defined.
According to a further aspect of the present invention a flexible flame-retardant polyurethane foam comprises the reaction product of a polymeric polyol and an organic polyisocyanate characterised in that the foam contains expandable graphite as hereinafter defined.
The conditions needed to produce a flexible foam will vary according to the reactants selected. A person of ordinary skill in the art will know whether to include additives eg a catalyst or a blowing agent and what reaction conditions are required. The molecular weights of the polymeric polyols used in flexible foam manufacture are usually from 1000 to 10,000, preferably from 3000 to 7000, with a functionality of up to 4, preferably 2 to 3. The functionality of the polyisocyanate is usually at least 2.
By "expandable graphite" is meant graphite containing one or more exfoliating agents such that considerable expansion will occur at high temperatures.
The foam-forming reaction mixture usually contains graphite in an amount such that there will be at least 10% by weight, preferably at least 15% by weight and advantageously at least 25% by weight of graphite in the final foam. The amount of graphite required will depend upon the degree of flame retardance required of the foam but usually the amount of graphite will not exceed 30% by weight in the final foam.
The graphite may comprise the sole flame-retardant additive in the foam-forming reaction mixture.
Alternatively, other flame-retardant ingredients, known per se, may be used in addition to the graphite. Examples of such ingredients include the hydrated aluminas (eg BACO* FRF 40) and halogen and/or phosphorus-containing compounds, or antimony oxides, or boron-containing compounds.
If desired, intumescent-generating ingredients, eg ammonium polyphosphates, may be included in the foam-forming reaction mixture.
Usually the foams produced according to the present invention will pass the burning test described in the British Standard specification No. 4735 September 1974. Usually the foams of the present invention are sufficiently flame-retardant that if used with selected textile cover materials the resulting combinations would pass the No. 4 crib test of the British Standard specification BS 5852: Part 2: 1982, preferably the No. 5 crib test, more preferably the No. 6 crib test and advantageously the No. 7 crib test. In view of the varying degree of flammability of different textile materials it is impossible to give absolute directions as to which textile materials are to be selected. However, a person of ordinary skill in the art would know which materials are likely to be suitable and simple trial and error would then establish whether they were indeed suitable. In order to prepare a foam capable of passing the No. 7 crib test it would generally be necessary for the amount of expendable graphite in the foam to be at least 25% by weight.
The present invention will be illustrated by way of the following Examples.
I: LOW RESILIENCE FOAMS EXAMPLES 1 TO 3
Free-rise, low-resilience polyurethane foams were made from the formulations shown in TABLE A (overleaf). (Quantities are parts by weight).
              TABLE A                                                     
______________________________________                                    
Ingredient                                                                
          CON-    CON-    EXAM-  EXAM-  EXAM-                             
(see notes                                                                
          TROL    TROL    PLE    PLE    PLE                               
below)    X       Y       1      2      3                                 
______________________________________                                    
Polymeric 100     100     100    100    100                               
polyol (a)                                                                
Water     0.8     0.8     0.8    0.8    0.8                               
Glycerol  2.5     2.5     2.5    2.5    2.5                               
Amine     2.3     2.3     2.3    2.3    2.3                               
catalyst (b)                                                              
Surfactant (c)                                                            
          0.67    0.67    0.67   0.67   0.67                              
Polybutene (d)                                                            
          17      17      17     8.5    8.5                               
Dimethyl  0.3     0.3     0.3    0.3    0.3                               
Ethanolamine                                                              
catalyst (e)                                                              
Alumina   --      40      --     --     --                                
hydrate (f)                                                               
Expandable                                                                
          --      --      40     20     --                                
Fine grade                                                                
graphite                                                                  
Expandable                                                                
          --      --      --     --     20                                
Coarse grade                                                              
graphite                                                                  
Blowing   --      --      5      5      5                                 
agent (g)                                                                 
Polyiso-  50      50      50     50     50                                
cyanate (h)                                                               
______________________________________                                    
 Notes to TABLE A                                                         
 (a) A polyether polyol, available from Lankro Chemicals Limited as G 1000
 (b) Triethylene diamine, available from Air Products Limited as DABCO 33 
 LV (DABCO is a Registered Trade Mark).                                   
 (c) A polyalkylene oxide polysiloxane silicone copolymer, available from 
 P Chemicals Limited as SC 246.                                           
 (d) Available from B P Chemicals Limited as HYVIS 5 (HYVIS is a Registere
 Trade Mark).                                                             
 (e) Dimethylethanolamine, available from Diamond Shamrock Limited as     
 PROPAMINE A: (PROPAMINE is a Registered Trade Mark).                     
 (f) Available from British Aluminium Co Limited as BACO FRF 40 (BACO is a
 Registered Trade Mark).                                                  
 (g) A fluorocarbon blowing agent, available from I.C.I. Limited as ARCTON
 11.                                                                      
 (h) A 20:80 mixture of methylenebis-2,4-phenyldiisocyanate (M.D.I.) and  
 tolylene diisocyanate (T.D.I.) available from B P Chemicals Limited as I 
 13-17.
Samples of each of the above foams were subjected to the burning tests described in British Standards Specification No 4735 and the results were as follows:
CONTROL X: Average burn length 125 mm in 121 seconds, i.e. the whole sample was burnt.
CONTROL Y: The addition of alumina hydrate gave only a slight improvement, the average burn length of this sample being 125 mm in 159 seconds.
EXAMPLE 1: Average burn length using 40 php fine-grade graphite was 38 mm in 113 seconds. The foam charred (as opposed to the foam of the two CONTROL examples which melted and dripped).
EXAMPLE 2: Reduction of the polybutene level and of the graphite level to 8.5 php and 20 php respectively led to an average burn length of 40 mm in 133 seconds.
EXAMPLE 3: Substitution of coarse-grade graphite (20 php) in the formulation of EXAMPLE 2 produced an average burn length of 42 mm in 120 seconds, i.e. not significantly different from that of EXAMPLE 2.
The formulations of CONTROL EXAMPLE X and of EXAMPLES 1 and 2 (above) were also moulded and the resultant mouldings tested according to British Standards Specification No. 2782, Method 141 (Oxygen Index Test). The following results were obtained:
______________________________________                                    
Example        Oxygen Index                                               
______________________________________                                    
CONTROL X      23.8                                                       
EXAMPLE 1      33                                                         
EXAMPLE 2      30.5                                                       
______________________________________
II: CONVENTIONAL FOAMS EXAMPLES 4 TO 6
Conventional polyurethane foams were made by moulding the formulations shown in TABLE B (below) followed by curing for 14 minutes at 150° C. (Quantities are parts by weight).
              TABLE B                                                     
______________________________________                                    
Ingredient   EXAM-       EXAM-    EXAM-                                   
(see notes   PLE         PLE      PLE                                     
below)       4           5        6                                       
______________________________________                                    
Polymeric polyol (a)                                                      
             600         600      600                                     
Water        7.5         7.5      7.5                                     
Amine catalyst (b)                                                        
             5           5        5                                       
N--ethylmorpholine                                                        
             3.5         3.5      3.5                                     
Surfactant (c)                                                            
             0.6         0.6      0.6                                     
Graphite (d) 120         120      240                                     
F.R. additive (e)                                                         
             --          60       --                                      
Polyisocyanate (f)                                                        
             115         115      115                                     
______________________________________                                    
 Notes to TABLE B                                                         
 (a) A polyoxyethylene/polyoxypropylene triol, of approximate molecular   
 weight 3500, having a high proportion of terminal primary hydroxyl groups
 (b) DABCO 33 LV (see TABLE A)                                            
 (c) SC246 (see TABLE A)                                                  
 (d) Fine grade expandable graphite.                                      
 (e) A material containing chlorine and phosphorus, available from Tenneco
 Organics Limited as TOLGARD V6 (TOLGARD is a Registered Trade Mark).     
 (f) An 80:20 mixture of the 2,4  and 2,6  isomers of tolylene diisocyanat
 (T.D.I.).
Samples of each of the above foams were tested according to the various crib tests described in British Standards Specification No. 5852, Part 2, the weights of the wooden cribs being as follows:
No. 4 crib: 8.5 g;
No. 5 crib: 17 g;
No. 6 crib: 60 g.
EXAMPLE 4: A No. 4 crib was placed directly on the top surface of the moulding and ignited.
Burning time of crib: 31/2 minutes
Flaming of foam ceased: 6 minutes
Progressive smouldering: None
EXAMPLE 5: As EXAMPLE 4, but with No. 5 crib.
Burning time of crib: 4 minutes
Flaming of foam ceased: 6 minutes
Progressive smouldering: None
EXAMPLE 6: As EXAMPLE 4, but with No. 6 crib.
Burning time of crib: 8 minutes
Flaming of foam ceased: 11 minutes
Progressive smouldering: None
III: HIGH-RESILIENCE FOAMS EXAMPLES 7 AND 8
High-resilience foams were made by moulding the formulations shown in TABLES C and D (below) in a mould at 50° C., followed by curing for 10 minutes at room temperature. (Quantities are parts by weight).
              TABLE C                                                     
______________________________________                                    
Ingredient                                                                
(see notes         EXAMPLE                                                
below)             7                                                      
______________________________________                                    
Polymeric polyol (a)                                                      
                   100                                                    
Water              2.5                                                    
Surfactant (b)     0.9                                                    
Amine catalyst (c) 1.2                                                    
Tertiary amine catalyst (d)                                               
                   0.2                                                    
Blowing agent (e)  10                                                     
Dibutyltin dilaurate                                                      
                   0.03                                                   
Graphite (f)       20                                                     
Chlorinated paraffin (g)                                                  
                   10                                                     
Polyisocyanate (h) 60                                                     
______________________________________                                    
 Notes to TABLE C                                                         
 (a) A polyoxypropylene polyoxyethylene triol of approximate molecular    
 weight 6000, having a high proportion of terminal primary hydroxyl groups
 and available from Bayer AG under the reference 7963.                    
 (b) A silicone surfactant, available from Goldschmidt AG under the       
 reference B8629.                                                         
 (c) DABCO 33 LV (see TABLE A)                                            
 (d) Available from Union Carbide under the reference Al                  
 (e) ARCTON 11 (see TABLE A)                                              
 (f) Fine grade expandable graphite                                       
 (g) Available from I.C.I. Limited as CERECLOR S52 (CERECLOR is a         
 Registered Trade Mark)                                                   
 (h) A modified MDI, available from I.C.I. Limited under the reference VM 
 25.
A sample of this foam was tested using a No. 5 crib.
Burning time of crib: 31/2 minutes
Flaming of foam ceased: 6 minutes
Emission of smoke ceased: 20 minutes
Progressive smouldering: None
              TABLE D                                                     
______________________________________                                    
Ingredient                                                                
(see notes            EXAMPLE                                             
below)                8                                                   
______________________________________                                    
Polymeric polyol (a)  100                                                 
Cross-linking agent (b)                                                   
                      6                                                   
Water                 8                                                   
Amine catalyst (c)    1.2                                                 
Tertiary amine catalyst (d)                                               
                      0.2                                                 
Surfactant (e)        0.9                                                 
Graphite (f)          20                                                  
Chlorine/phosphorus compound (g)                                          
                      10                                                  
Dibutyl tin dilaurate 0.03                                                
Polyisocyanate (h)    41.5                                                
______________________________________                                    
 Notes to TABLE D                                                         
 (a) Polyol 7963 (See TABLE C)                                            
 (b) Available from Lankro Chemicals Limited under the reference A260     
 (c) DABCO 33 LV (see TABLE A)                                            
 (d) Al (see TABLE C)                                                     
 (e) B8629 (see TABLE C)                                                  
 (f) Fine grade expandible graphite                                       
 (g) TOLGARD V6 (see TABLE B)                                             
 (h) I 13-17 (see TABLE A)
A sample of this foam was also tested using a No. 5 crib.
Burning time of crib: 5 minutes
Emission of smoke ceased: 13 minutes
Progressive smouldering: None
EXAMPLES 9 AND 10
High-resilience foams were made by including formulations as shown in Table E in a mould at 45° C. followed by curing for 10 minutes at room temperature. (Quantities are parts by weight).
              TABLE E                                                     
______________________________________                                    
Ingredient          Examples 9 and 10                                     
______________________________________                                    
Polymeric polyol (a)                                                      
                    50                                                    
Polymeric polyol (b)                                                      
                    50                                                    
Water               3.2                                                   
Amine catalyst (c)  3                                                     
Tertiary Amine Catalyst (d)                                               
                    0.2                                                   
Surfactant (e)      0.6                                                   
Expandable graphite 43.7                                                  
Sodium tetra borate decahydrate                                           
                    5                                                     
Polyisocyanate (f)  75                                                    
______________________________________                                    
 Notes to Table E                                                         
 (a) A polyoxypropylene polyoxyethylene triol of approximate molecular    
 weight 6000, having a high proportion of terminal primary hydroxyl groups
 and available from Bayer AG under the reference 7963.                    
 (b) Available from B P Chemical Limited under the reference U1315        
 (c) Triethylene diamine, available from Air Products Limited as DABCO 33L
 (d) Available from Union Carbide under the reference NiAX A1             
 (e) Polyalkylene oxide polydimethyl siloxane silicone available under the
 reference B4113                                                          
 (f) Modified diphenyl methane diisocyanate available from ICI under      
 reference VM25.
For Example 9, foam was tested in combination with a woollen fabric of weight approximately 400 g/m2 using a No. 6 wooden crib (weight 60 g) according to BS 5852 Part 2, 1982. Flaming of the foam/fabric combination ceased 11.5 minutes from the ignition of the wooden crib and there was no progressive smouldering revealed by examination one hour after ignition. The weight loss shown by the foam component was about 3%.
For Example 10, foam was tested in combination with a wool moquette fabric of weight approximately 800 g/m2 using a No. 7 wooden crib (weight 120 g) according to BS 5852 Part 2 1982. Flaming of the foam/fabric combination ceased 15 minutes from ignition of the crib. There was no progressive smouldering.
EXAMPLE 11
A conventional polyether polyurethane foam, similar to those described in EXAMPLES 4 to 6 but containing 30% by weight of graphite and having a foam density of 36 Kg/m3, was tested in the F.A.A. Kerosene Burner Test* in combination with a 100% wool face fabric and a partially-carbonised viscose interliner. It was found that this combination self-extinguished 3.5 minutes after the commencement of the test and that the overall weight loss was 6.8%.

Claims (12)

What is claimed is:
1. A method for the production of a flexible, flame-retardant polyurethane foam by reacting in a foam-forming reaction mixture a polymeric polyol, an organic polyisocyanate and an effective amount of expandable graphite, wherein said expandable graphite contains one or more exfoliating agents.
2. The method of claim 1, wherein the amount of said expandable graphite in said foam-forming reaction mixture is such that the resulting foam contains at least 10% by weight of said expandable graphite.
3. The method of claim 1, wherein the amount of said graphite in said foam-forming reaction mixture is such that the resulting foam contains at least 15% by weight of said expandable graphite.
4. The method of claim 1, wherein the amount of said graphite in said foam-forming reaction mixture is such that the resulting foam contains at least 25% by weight of said expandable graphite.
5. The method of claim 1, wherein said foam-forming reaction mixture also contains a flame-retardant ingredient selected from the group consisting of hydrated aluminas, halogen-containing compounds, phosphorous-containing compounds, compounds containing halogen and phosphorous, antimony oxides and boron compounds.
6. The method of claim 1, wherein said foam-forming reaction mixture also contains an intumescing ingredient.
7. The method of claim 6, wherein said intumescing ingredient is an ammonium polyphosphate.
8. A flexible, flame-retardant polyurethane foam, said foam being the reaction product under foam-forming conditions of a polymeric polyol, an organic polyisocyanate and an effective amount of expandable graphite, said expandable graphite containing one or moe exfoliating agents.
9. The foam of claim 8 which passes the burning test of British Standard Specification No. 4735, September 1974.
10. The foam of claim 8 which when used in combination with a textile cover passes the No. 7 crib test of British Standard Specification No. 5852, Part 2, 1982.
11. The foam of claim 1 wherein the polymeric polyol is a polyether polyol.
12. The foam of claim 8 wherein said foam is the reaction product under foam-forming conditions of a polyether polyol, an organic polyisocyanate and an effective amount of expandable graphite, said expandable graphite containing one or more exfolidating agents.
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US4871477A (en) * 1983-02-15 1989-10-03 Firestop Chemical Corporation Fire protected foamed polymeric materials
US4931479A (en) * 1988-11-07 1990-06-05 Chomerics, Inc. Foam in place conductive polyurethane foam
US4945015A (en) * 1986-09-17 1990-07-31 Dixon International Limited Intumescent material
WO1990009271A1 (en) * 1989-02-16 1990-08-23 Dow Mitsubishi Kasei Limited Production of flame-retardant rebonded foam
US4999385A (en) * 1989-07-13 1991-03-12 The Dow Chemical Company Carbonaceous foams
US5162394A (en) * 1990-09-18 1992-11-10 501 Chemco Inc. Fire-retardant chemical compositions
US5173515A (en) * 1989-05-30 1992-12-22 Bayer Aktiengesellschaft Fire retardant foams comprising expandable graphite, amine salts and phosphorous polyols
US5223324A (en) * 1988-01-29 1993-06-29 The Dow Chemical Company Flame retardant foams
US5395860A (en) * 1992-08-14 1995-03-07 Arco Chemical Technology, L.P. Flexible polyurethane foams using chlorinated alkanes
GB2299584A (en) * 1995-04-03 1996-10-09 Metzeler Kay Ltd Flame retardant flexible polymer foam
US5650448A (en) * 1995-04-03 1997-07-22 Kay-Metzeler Limited Flame retardant flexible foam
US5876134A (en) * 1992-02-14 1999-03-02 The Gillette Company Foam grip
US5952248A (en) * 1997-12-11 1999-09-14 Horton; Bill D. Fire retardant thermal and acoustic insulation material
EP0953625A1 (en) * 1998-04-27 1999-11-03 Colux Gesellschaft für Licht- und Leichtbau mbH Use of a two-compartment aerosol container and a fire retardant construction foam
US6017987A (en) * 1995-03-03 2000-01-25 Tosoh Corporation Fire-retardant polymer composition
WO2000046283A1 (en) * 1999-02-02 2000-08-10 The Dow Chemical Company Open-celled semi-rigid foams with exfoliating graphite
US6197869B1 (en) 1996-05-30 2001-03-06 Basf Aktiengesellschaft Non-flammable, thermoplastic moulded materials with improved anti-drip properties
US6245842B1 (en) 2000-03-03 2001-06-12 Trus Joist Macmillan A Limited Partnership Flame-retardant coating and building product
WO2001010182A3 (en) * 1999-07-30 2001-08-16 Amesbury Group Inc Method and apparatus for manufacturing a flame retardant emi gasket
EP1153066B1 (en) * 1999-02-02 2003-04-09 Dow Global Technologies Inc. Open-celled polyurethane foams containing graphite which exhibit low thermal conductivity
US20040122119A1 (en) * 2000-03-27 2004-06-24 Burgess James H. Fire resistant foam and foam products, method and dispersions for making same
WO2004052152A1 (en) 2002-12-11 2004-06-24 Kay-Metzeler Limited Cushion for an aircraft seat
US20050095936A1 (en) * 2004-09-02 2005-05-05 Jones Walter G. Upholstery panels with fire resistant backing layer
US20060210787A1 (en) * 2005-03-18 2006-09-21 Alberto Veneruso Structure stuffed with melamine and polyurethane foam
US20060211784A1 (en) * 2005-03-18 2006-09-21 Alberto Veneruso Polyurethane foam with improved properties and stuffed structure comprised of said foam
WO2006125258A1 (en) * 2005-05-24 2006-11-30 Pacific Brands Household Products Pty Ltd Low resilience flame retardant polyurethane foam
US20070011693A1 (en) * 2005-02-09 2007-01-11 Creasy Larry D Jr Flame retardant EMI shields
WO2007050000A1 (en) * 2005-10-26 2007-05-03 Industrial Property Of Scandinavia Ab Fire-resistant composition for coating, sealing and protection purposes
US7393879B1 (en) 2002-06-06 2008-07-01 Chestnut Ridge Foam, Inc. High resilient silicone foam and process for preparing same
US20080157915A1 (en) * 2007-01-03 2008-07-03 Ethan Lin Flame retardant, electrically-conductive pressure sensitive adhesive materials and methods of making the same
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US20100183856A1 (en) * 2008-12-15 2010-07-22 David Kind Elastomeric body with elastic fire retardant coating
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US20110060064A1 (en) * 2008-04-01 2011-03-10 Metzeler Schaum Gmbh Flame-retardant, reduced-weight elastic flexible polyurethane foam
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Cited By (51)

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US4871477A (en) * 1983-02-15 1989-10-03 Firestop Chemical Corporation Fire protected foamed polymeric materials
US4945015A (en) * 1986-09-17 1990-07-31 Dixon International Limited Intumescent material
US5223324A (en) * 1988-01-29 1993-06-29 The Dow Chemical Company Flame retardant foams
US4857394A (en) * 1988-01-29 1989-08-15 The Dow Chemical Company Flame retardant foams
US4931479A (en) * 1988-11-07 1990-06-05 Chomerics, Inc. Foam in place conductive polyurethane foam
WO1990009271A1 (en) * 1989-02-16 1990-08-23 Dow Mitsubishi Kasei Limited Production of flame-retardant rebonded foam
US5173515A (en) * 1989-05-30 1992-12-22 Bayer Aktiengesellschaft Fire retardant foams comprising expandable graphite, amine salts and phosphorous polyols
US4999385A (en) * 1989-07-13 1991-03-12 The Dow Chemical Company Carbonaceous foams
US5162394A (en) * 1990-09-18 1992-11-10 501 Chemco Inc. Fire-retardant chemical compositions
US5876134A (en) * 1992-02-14 1999-03-02 The Gillette Company Foam grip
US5395860A (en) * 1992-08-14 1995-03-07 Arco Chemical Technology, L.P. Flexible polyurethane foams using chlorinated alkanes
US6017987A (en) * 1995-03-03 2000-01-25 Tosoh Corporation Fire-retardant polymer composition
US5719199A (en) * 1995-04-03 1998-02-17 Kay-Metzeler Limited Flame retardant flexible foam
GB2299584B (en) * 1995-04-03 1998-11-04 Metzeler Kay Ltd Flame retardent flexible foam
US5650448A (en) * 1995-04-03 1997-07-22 Kay-Metzeler Limited Flame retardant flexible foam
GB2299584A (en) * 1995-04-03 1996-10-09 Metzeler Kay Ltd Flame retardant flexible polymer foam
US6197869B1 (en) 1996-05-30 2001-03-06 Basf Aktiengesellschaft Non-flammable, thermoplastic moulded materials with improved anti-drip properties
US5952248A (en) * 1997-12-11 1999-09-14 Horton; Bill D. Fire retardant thermal and acoustic insulation material
EP0953625A1 (en) * 1998-04-27 1999-11-03 Colux Gesellschaft für Licht- und Leichtbau mbH Use of a two-compartment aerosol container and a fire retardant construction foam
US6602925B1 (en) 1999-02-02 2003-08-05 Dow Global Technologies Inc. Open-celled polyurethane foams containing graphite which exhibit low thermal conductivity
EP1153066B1 (en) * 1999-02-02 2003-04-09 Dow Global Technologies Inc. Open-celled polyurethane foams containing graphite which exhibit low thermal conductivity
US6552098B1 (en) 1999-02-02 2003-04-22 Dow Global Technologies Inc. Open-celled semi-rigid foams with exfoliating graphite
WO2000046283A1 (en) * 1999-02-02 2000-08-10 The Dow Chemical Company Open-celled semi-rigid foams with exfoliating graphite
WO2001010182A3 (en) * 1999-07-30 2001-08-16 Amesbury Group Inc Method and apparatus for manufacturing a flame retardant emi gasket
US6245842B1 (en) 2000-03-03 2001-06-12 Trus Joist Macmillan A Limited Partnership Flame-retardant coating and building product
US7435762B2 (en) 2000-03-27 2008-10-14 Ip Rights, Llc Fire resistant foam and foam products, method and dispersions for making same
US20040122119A1 (en) * 2000-03-27 2004-06-24 Burgess James H. Fire resistant foam and foam products, method and dispersions for making same
US7393879B1 (en) 2002-06-06 2008-07-01 Chestnut Ridge Foam, Inc. High resilient silicone foam and process for preparing same
WO2004052152A1 (en) 2002-12-11 2004-06-24 Kay-Metzeler Limited Cushion for an aircraft seat
US9850429B2 (en) * 2004-07-22 2017-12-26 Compart Sas Firestop material
US20050095936A1 (en) * 2004-09-02 2005-05-05 Jones Walter G. Upholstery panels with fire resistant backing layer
US20100258344A1 (en) * 2005-02-09 2010-10-14 Laird Technologies, Inc. Flame retardant emi shields
US20070011693A1 (en) * 2005-02-09 2007-01-11 Creasy Larry D Jr Flame retardant EMI shields
US8545974B2 (en) 2005-02-09 2013-10-01 Laird Technologies, Inc. Flame retardant EMI shields
US20060210787A1 (en) * 2005-03-18 2006-09-21 Alberto Veneruso Structure stuffed with melamine and polyurethane foam
US20060211784A1 (en) * 2005-03-18 2006-09-21 Alberto Veneruso Polyurethane foam with improved properties and stuffed structure comprised of said foam
AU2006251857B2 (en) * 2005-05-24 2011-04-07 Australian Comfort Group Pty. Ltd. Low resilience flame retardant polyurethane foam
WO2006125258A1 (en) * 2005-05-24 2006-11-30 Pacific Brands Household Products Pty Ltd Low resilience flame retardant polyurethane foam
US20090036561A1 (en) * 2005-10-26 2009-02-05 Sune Bertil Nygren Fire-resistant composition for coating, sealing and protection purposes
WO2007050000A1 (en) * 2005-10-26 2007-05-03 Industrial Property Of Scandinavia Ab Fire-resistant composition for coating, sealing and protection purposes
US20080157915A1 (en) * 2007-01-03 2008-07-03 Ethan Lin Flame retardant, electrically-conductive pressure sensitive adhesive materials and methods of making the same
US20120029103A1 (en) * 2007-05-07 2012-02-02 Ceram Polymerik Pty Ltd Polymer foam and foam articles for fire protection
US8889754B2 (en) * 2007-05-07 2014-11-18 Polymers Crc Ltd Polymer foam and foam articles for fire protection
US20100305226A1 (en) * 2007-06-20 2010-12-02 Wacker Chemie Ag Polyurethane foam containing silicone
DE102007028253A1 (en) 2007-06-20 2008-12-24 Wacker Chemie Ag Silicone-containing polyurethane foam
US20110060064A1 (en) * 2008-04-01 2011-03-10 Metzeler Schaum Gmbh Flame-retardant, reduced-weight elastic flexible polyurethane foam
US20100183856A1 (en) * 2008-12-15 2010-07-22 David Kind Elastomeric body with elastic fire retardant coating
US9745434B2 (en) 2008-12-15 2017-08-29 Trelleborg Industrial Products Uk Ltd Elastomeric body with elastic fire retardant coating
WO2017161207A1 (en) 2016-03-16 2017-09-21 Rco Engineering Inc. Improved system and process for the manufacture of polymer foam with additives
CN112979914A (en) * 2021-03-11 2021-06-18 吉林省金越交通装备股份有限公司 Graphite-filled high-efficiency flame-retardant high-resilience polyurethane sponge and preparation method thereof
US20220410528A1 (en) * 2021-06-28 2022-12-29 Saint-Gobain Performance Plastics Corporation Multilayer composite with thermal barrier properties

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EP0192888B1 (en) 1993-10-06
GB8529303D0 (en) 1986-01-02
GB8432153D0 (en) 1985-01-30
ZA859284B (en) 1987-07-29
DE3587618T2 (en) 1994-03-10
DE3587618D1 (en) 1993-11-11
EP0192888A3 (en) 1986-11-20
EP0192888A2 (en) 1986-09-03
GB2168706B (en) 1987-10-21
HK90194A (en) 1994-09-09
GB2168706A (en) 1986-06-25

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